When.com Web Search

  1. Ad

    related to: 2 carboxylic acids put together makes a product

Search results

  1. Results From The WOW.Com Content Network
  2. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    The Kolbe reaction is formally a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions). The overall reaction is: If a mixture of two different carboxylates are used, all combinations of them are generally seen as the organic product structures: 3 R 1 COO − + 3 R 2 COO − → R 1 −R 1 + R 1 −R 2 + R 2 −R 2 + 6 CO 2 ...

  3. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  4. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group (−C(=O)−OH) [1] attached to an R-group. The general formula of a carboxylic acid is often written as R−COOH or R−CO 2 H, sometimes as R−C(O)OH with R referring to an organyl group (e.g., alkyl, alkenyl, aryl), or hydrogen, or other groups ...

  5. Decarboxylative cross-coupling - Wikipedia

    en.wikipedia.org/wiki/Decarboxylative_cross-coupling

    They employed propiolic acid as an alkyne source. One year later, S. Lee applied the decarboxylative coupling reactions toward 2-octynoic acid and phenylpropiolic acid. In 2010, Xue et al. reported the coupling of an aryl halide and alkynyl carboxylic acid under mild reactions conditions and a copper-only catalyst to obtain aryl alkynes.

  6. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O. Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  7. Carboxylation - Wikipedia

    en.wikipedia.org/wiki/Carboxylation

    Carboxylation is a chemical reaction in which a carboxylic acid is produced by treating a substrate with carbon dioxide. [1] The opposite reaction is decarboxylation.In chemistry, the term carbonation is sometimes used synonymously with carboxylation, especially when applied to the reaction of carbanionic reagents with CO 2.

  8. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    Adding boric acid to the acid-catalyzed reaction mixture increases the yield of phenol product over phenyl carboxylic acid product, even when using phenyl aldehyde or ketone reactants with electron-donating groups meta to the carbonyl group or electron-withdrawing groups ortho or para to the carbonyl group. Boric acid and hydrogen peroxide form ...

  9. Ketonic decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Ketonic_decarboxylation

    Ketonic decarboxylation (also known as decarboxylative ketonization) is a type of organic reaction and a decarboxylation converting two equivalents of a carboxylic acid (R−C(=O)OH) to a symmetric ketone (R 2 C=O) by the application of heat. It can be thought of as a decarboxylative Claisen condensation of two identical molecules.